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Correlated changes in structure and viscosity during gelatinization and gelation of tapioca starch granules.
Huang, Hsien-Kai; Sheu, Hwo-Shuenn; Chuang, Wei-Tsung; Jeng, U-Ser; Su, An-Chung; Wu, Wei-Ru; Liao, Kuei-Fen; Chen, Chun-Yu; Chang, Shing-Yun; Lai, Hsi-Mei.
Affiliation
  • Huang HK; Department of Chemical Engineering, National Tsing Hua University, Hsinchu 300, Taiwan.
  • Sheu HS; National Synchrotron Radiation Research Center, Hsinchu 300, Taiwan.
  • Chuang WT; National Synchrotron Radiation Research Center, Hsinchu 300, Taiwan.
  • Jeng US; Department of Chemical Engineering, National Tsing Hua University, Hsinchu 300, Taiwan ; National Synchrotron Radiation Research Center, Hsinchu 300, Taiwan.
  • Su AC; Department of Chemical Engineering, National Tsing Hua University, Hsinchu 300, Taiwan.
  • Wu WR; National Synchrotron Radiation Research Center, Hsinchu 300, Taiwan.
  • Liao KF; National Synchrotron Radiation Research Center, Hsinchu 300, Taiwan.
  • Chen CY; National Synchrotron Radiation Research Center, Hsinchu 300, Taiwan.
  • Chang SY; Department of Agricultural Chemistry, National Taiwan University, Taipei 106, Taiwan.
  • Lai HM; Department of Agricultural Chemistry, National Taiwan University, Taipei 106, Taiwan.
IUCrJ ; 1(Pt 6): 418-28, 2014 Nov 01.
Article in En | MEDLINE | ID: mdl-25485122
Melting of native tapioca starch granules in aqueous pastes upon heating is observed in situ using simultaneous small- and wide-angle X-ray scattering (SAXS/WAXS) and solution viscometry. Correlated structure and viscosity changes suggest closely associated amylose and amylopectin chains in the semicrystalline layers, and the release of amylose chains for enhanced solution viscosity occurs largely after melting of the semicrystalline structure. Before melting, WAXS results reveal mixed crystals of A- and B-types (∼4:1 by weight), whereas SAXS results indicate that the semicrystalline layers are composed of lamellar blocklets of ca 43 nm domain size, with polydisperse crystalline (≃7.5 nm) and amorphous (≃1.1 nm) layers alternatively assembled into a lamellar spacing of ≃8.6 nm with 20% polydispersity. Upon melting, the semicrystalline lamellae disintegrate into disperse and molten amylopectin nanoclusters with dissolved and partially untangled amylose chains in the aqueous matrix which leads to increased solution viscosity. During subsequent cooling, gelation starts at around 347 K; successively increased solution viscosity coincides with the development of nanocluster aggregation to a fractal dimension ≃2.3 at 303 K, signifying increasing intercluster association through collapsed amylose chains owing to decreased solvency of the aqueous medium with decreasing temperature.
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